| Literature DB >> 11208083 |
Abstract
Three-dimensional time-lapse (4D) fluorescence microscopy is becoming a routine experimental tool. This article summarizes current technologies, and describes a new method for speeding image acquisition during 4D confocal microscopy.Mesh:
Year: 2000 PMID: 11208083
Source DB: PubMed Journal: Traffic ISSN: 1398-9219 Impact factor: 6.215